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首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Effect of ultrasonicated carboxymethylglucan on cyclophosphamide induced mutagenicity.
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Effect of ultrasonicated carboxymethylglucan on cyclophosphamide induced mutagenicity.

机译:超声羧甲基葡聚糖对环磷酰胺诱导的致突变性的影响。

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摘要

Carboxymethylglucan (CMG) with ultrasonically lowered molecular weight (0.89 x 10(5)) was administered either intraperitoneally, intravenously or orally prior to cyclophosphamide (CP) injection and its effect on the frequency of micronuclei in mouse bone marrow was evaluated. Both parenteral (intraperitoneal and intravenous) and oral administration of CMG decreased the clastogenic effect of CP. The protective effect induced by intravenous and intraperitoneal administration was concentration-dependent, with a higher decrease achieved by 200 mg/kg than by 100 mg/kg body weight. With the lower dose of CMG a 2-h interval was necessary between intravenous CMG administration and CP injection. Oral pretreatment of mice with CMG decreased statistically significantly the frequency of micronuclei in polychromatic erythrocytes of the bone marrow. The fact that ultrasonically depolymerized CMG was effective also on oral administration is indicative of the passage of smaller CMG molecules through the wall of the gastrointestinal tract.
机译:在注射环磷酰胺(CP)之前,通过腹膜内,静脉内或口服给予具有超声波降低分子量(0.89 x 10(5))的羧甲基葡聚糖(CMG),并评估其对小鼠骨髓中微核频率的影响。肠胃外(腹膜内和静脉内)和口服CMG均可降低CP的致盲作用。静脉和腹膜内给药所引起的保护作用是浓度依赖性的,与100 mg / kg体重相比,200 mg / kg的降低幅度更大。对于较低的CMG剂量,静脉内CMG注射和CP注射之间必须间隔2小时。口服CMG小鼠预处理在统计学上显着降低了骨髓多色红细胞中微核的频率。超声解聚的CMG对口服给药也有效,这一事实表明较小的CMG分子可通过胃肠道壁。

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